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Rizatriptan Benzoate - 65862-625-90 - (Rizatriptan Benzoate)

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Drug Information of Rizatriptan Benzoate

Product NDC: 65862-625
Proprietary Name: Rizatriptan Benzoate
Non Proprietary Name: Rizatriptan Benzoate
Active Ingredient(s): 5    mg/1 & nbsp;   Rizatriptan Benzoate
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of Rizatriptan Benzoate

Product NDC: 65862-625
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA203062
Marketing Category: ANDA
Start Marketing Date: 20130701

Package Information of Rizatriptan Benzoate

Package NDC: 65862-625-90
Package Description: 3 BLISTER PACK in 1 CARTON (65862-625-90) > 3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (65862-625-03)

NDC Information of Rizatriptan Benzoate

NDC Code 65862-625-90
Proprietary Name Rizatriptan Benzoate
Package Description 3 BLISTER PACK in 1 CARTON (65862-625-90) > 3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (65862-625-03)
Product NDC 65862-625
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Rizatriptan Benzoate
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20130701
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name RIZATRIPTAN BENZOATE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]

Complete Information of Rizatriptan Benzoate


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